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临床试验/NCT00486681
NCT00486681已完成不适用

Evaluation of the Implementation of the Accu-Chek Inform Cobas IT 1000 System in Three Medical Hospital Departments: Impact on the Management of Diabetes

University Hospital, Grenoble1 个研究点 分布在 1 个国家目标入组 949 人开始时间: 2007年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
949
试验地点
1
主要终点
compare glycemic control of patients hospitalized in 3 departments

研究概览

简要总结

The principal objective of this single-center 2-period study is to evaluate the glycemic control of in-patients in 3 hospital departments (Diabetology, Cardiology and Pulmonary Care) as the rate of capillary blood glucose measurements within a pre-define target range, and to compare results during the period I (warning of the Accu-Check Inform glucose meter on glucose levels not activated) and period II (warning activated).

详细描述

The study is a 6-month large scale assessment of an information system consisting in a glucose meter with multiple alerts (Accu-Chek Inform) associated with a data base (Cobas IT 1000) in order to share the results of glucose monitoring using the hospital information network.

The appraisal of the glycemic control was based on the rate of capillary blood glucose measurements within a pre-defined target range (3.9-8.5 mMol/l) during each study period.

Whether the system implementation can improve the outcome related to the management of in-patients with diabetes is assessed in 3 hospital departments (Diabetology, Cardiology and Pulmonary Care) as follows:

  • principal objective, glycemic control of in-patients (Cardiology and Pulmonary Care) as the rate of capillary blood glucose (CBG) values within the pre-defined target range, and comparison of results observed during period I (meter warning not activated) and period II (warning of the meter on out-of-target glucose level activated).
  • the impact on the performance of quality controls of CBG measurements with (period II) or without (period I) activation of a warning on the meter related to inappropriate quality control frequency (all departments).
  • evaluate the traceability of CBG results and compare it with (period II) or without (period I) the activation of the automatic record of data ensured by the Accu-Chek Inform meter and Cobas IT 1000 data base (all departments).
  • during a sub-period of period II, the impact on patient glycemic control of the intervention of a diabetologist, determined by the activation of a warning sent to the physician in case of out of target CBG results via the Cobas IT 1000 data base (Cardiology and Pulmonary Care).
  • the impact of the above warning activation plus diabetologist intervention on the incidence of low CBG.

研究设计

研究类型
Observational
观察模型
Case Crossover
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • In-patients,
  • Age > 18 years,
  • Requiring a monitoring of capillary blood glucose levels

排除标准

  • No glucose monitoring needed

结局指标

主要结局

compare glycemic control of patients hospitalized in 3 departments

时间窗: hospitalisation period

次要结局

  • number of glycemia controls(hospitalisation period)
  • number of traceable glycemia readings(hospitalisation period)
  • number of hypoglycemia events and frequency of measures taken(hospitalisation period)
  • mean of % of glycemia for patients in warning phase with or without diabetologist intervention(hospitalisation period)

研究者

发起方
University Hospital, Grenoble
申办方类型
Other

研究点 (1)

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